Validation manager Jobs in Los Angeles, CA
Last updated: 6 hours ago
Southern California's Scientific community.We are currently looking for a.Greater Los Angeles area contract development and manufacturing organization.
Draft and Review User Requirement Specific...Show moreLast updated: 3 days ago
Role : CSV ProfessionalDuration : 6 MonthsOnsite / Hybrid / Remote : Fully OnsiteRate : OpenMy Client is seeking a skilled CSV professional with 8-10 years of experience in Computer System Validation (CSV)...Show moreLast updated: 6 hours ago
For over 15 years Trilyon has been at the forefront of providing comprehensive global workforce solutions and staffing services.
Leveraging our extensive expertise across multiple domains such as Cl...Show moreLast updated: 8 days ago
We anticipate the application window for this opening will close on - 21 Feb 2025.At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare acce...Show moreLast updated: 2 days ago
Enhance and Optimize Cleaning Validation Protocols.Develop, review, and refine cleaning validation protocols, reports, and SOPs to ensure compliance with GMP and global regulatory standards.Establi...Show moreLast updated: 4 days ago
Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry.Establis...Show moreLast updated: 22 days ago
Since 1973, East West Bank has served as a pathway to success.With over 110 locations across the U.Asia, we are the premier financial bridge between the East and West.
Our teams of experienced, mult...Show moreLast updated: 26 days ago
East West Bank is seeking a Model Validation Analyst to join the Bank’s Model Risk Management (MRM) group.The Model Validation Analyst will be responsible for helping to maintain, improve and execu...Show moreLast updated: 28 days ago
Support the Model Risk Manager in leading the validation team in producing value-added validation of the Bank’s models.Provide guidance to analysts in validation activities, such as developing test...Show moreLast updated: 11 days ago
Managing activities related to equipment, facilities, utility qualification, process, and cleaningvalidation.Responsibilities for the Sr Validation Manager.
Manage and execute equipment, facility, u...Show moreLast updated: 30+ days ago
Enhance and Optimize Cleaning Validation Protocols.Develop, review, and refine cleaning validation protocols, reports, and SOPs to ensure compliance with GMP and global regulatory standards.Establi...Show moreLast updated: 11 days ago
PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all appl...Show moreLast updated: 11 days ago
Eastridge Workforce Solutions is proud to partner with a leading pharmaceutical company in Lynwood, CA, in its search for a.
This is a direct hire opportunity offering excellent potential for growth...Show moreLast updated: 11 days ago
Position : Senior Validation Engineer (CSV).Location : LA Metro Area, CA (100% Onsite).At least 10 years of experience in Computer System Validation role in the regulated industry.Working knowledge o...Show moreLast updated: 3 days ago
- Promoted
Validation Engineer
BioPhase SolutionsLos Angeles, CA, US$100,000.00–$115,000.00 yearly
Full-time
- Promoted
- New!
Senior Validation Specialist
MasterCompliance LLCLos Angeles, CA, United StatesFull-time
- Promoted
Validation Engineer - Junior US
Trilyon, Inc.Santa Clara County, California, USAFull-time
- Promoted
Sr System Verification and Validation Engineer
MedtronicNorthridge, CA, United States$104,800.00–$157,200.00 yearly
Full-time
Sr Validation Manager - Lynwood CA
Zachary Piper SolutionsLynwood, CA, US Managing activities related to equipment, facilities, utility qualification, process, and cleaningvalidation.Responsibilities for the Sr Validation Manager.
Manage and execute equipment, facility, u...Show moreLast updated: 30+ days ago
- Promoted
Validation Specialist
SciPro Inc.Los Angeles, CA, United StatesTemporary
- Promoted
Validation Engineer
ValspecLos Angeles, CA, US$75,000.00–$95,000.00 yearly
Full-time
- Promoted
Model Validation Analyst
UnavailablePasadena, CA, United States$105,000.00 yearly
Full-time
Model Validation Analyst
East West BankPasadena, CA, US$130,000.00 yearly
Full-time
- Promoted
Sr. Model Validation Associate III
Bank of HopeLos Angeles, CA, United States$210,000.00 yearly
Full-time
- Promoted
Sr Validation Manager - Lynwood CA
Piper CompaniesLynwood, CAFull-time
- Promoted
Validation Specialist
SciProLos Angeles, CA, United StatesTemporary
QA Validation Manager
MarkenInglewood, California Manager is responsible for the oversight and implementation of the Marken Quality Management System (QMS), Marken Standard Operating Procedures (SOPs), processes, and policies required to manage va...Show moreLast updated: 30+ days ago
- Promoted
Validation Engineer
PSC BiotechLos Angeles, CA, United States$85,000.00–$100,000.00 yearly
Full-time
- Promoted
Validation Engineer
EastridgeLynwood, CA, USPermanent
- Promoted
Senior Validation Engineer (CSV)
Conrelv Solutions IncLos Angeles, CA, USFull-time
Validation Engineer
Katalyst HealthCares & Life SciencesLos Angeles, CA Develop and execute validation protocols for chambers, biosafety cabinets, utilities, and laboratory systems (including PCR systems, spectrophotometers, and cell counters).Generate comprehensive re...Show moreLast updated: 30+ days ago
Validation Engineer
BioPhase SolutionsLos Angeles, CA, US3 days ago
Salary
$100,000.00–$115,000.00 yearly
Job type
- Full-time
Job descriptionBachelors in engineering, chemistry, or related field Certifications related to GMP compliance, quality systems, or validation preferred. 1–3+ years of experience in validation engineering or a closely related field in a cGMP-regulated pharma or biotech environment. Strong working knowledge of process validation, equipment qualification (IQ / OQ / PQ), and pharmaceutical manufacturing processes. Proficiency in drafting and reviewing validation documents (URS, SOPs, protocols, reports). Familiarity with deviation investigations, CAPA processes, and audit responses. Basic vendor management skills to evaluate and coordinate with external equipment / service providers. Competence in using data analysis tools and MS Office applications to track and report validation results.
Job Description
Job Description
BioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a Validation Engineer to work for a leading Greater Los Angeles area contract development and manufacturing organization.
Salary : $100-115k+ / year depending on experience
Responsibilities :
- Draft and Review User Requirement Specifications (URS) : Develop and refine URS for new and existing process equipment, ensuring alignment with manufacturing needs and regulatory standards.
- Perform Equipment Qualifications (IQ, OQ, PQ) : Plan, execute, and document qualification protocols to verify equipment performance meets cGMP requirements and intended use.
- Execute Process Validation and Cleaning Validation : Identify critical process parameters, establish validation protocols, and conduct cleaning validations to maintain product quality and regulatory compliance.
- Generate and Maintain Validation Documentation : Prepare, review, and archive validation reports, SOPs, protocols, and related records to ensure clear traceability and audit readiness.
- Troubleshoot and Investigate Deviations : Collaborate with cross-functional teams to diagnose equipment and process issues, implement corrective actions (CAPA), and address audit observations promptly.
- Support Scale-Up and Technology Transfer Efforts : Work with manufacturing and development groups to optimize processes, facilitate seamless scale-up, and transfer validated methods across company sites.
- Coordinate with Cross-Functional Teams : Engage Quality, Process Development, and Manufacturing teams to meet project timelines, drive continuous improvement, and uphold cGMP standards.
Experience / Requirements :
Please send resumes to [email protected] and visit our website at www.biophaseinc.com for additional job opportunities!!!